Well Lead Medical Co., Ltd.
Well Lead Medical Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2025, with 1 FDA device recall on record.
Top product codes for Well Lead Medical Co., Ltd.
FDA recalls by Well Lead Medical Co., Ltd.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Well Lead Medical Co., Ltd.
- K241734 — Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter Compact
- K220722 — PVC Hydrophilic Urethral Catheter
- K220036 — Wellead Ureteral Catheter
- K211543 — Wei Nasal Jet Tube
- K211814 — Wellead Endoscopic Seal
- K202134 — Well Lead All Silicone Foley Catheter with Temperature Sensor
- K203119 — ClearPetra Suction-Evacuation Sheath
- K182739 — Endotracheal Tube with Evacuation Lumen
- K162340 — Stomach Tube
- K160801 — Well Lead Extraction Bag
- K161110 — ClearPetra Suction-Evacuation Sheath
- K151084 — Well Lead Ureteral Access Sheath
- K140667 — WELL LEAD HYDROPHILIC SILICONE FOLEY CATHETER
- K142563 — Well Lead PVC Urethral Catheter
- K133615 — WELL LEAD PVC HYDROPHILIC URETHRAL CATHETER
- K110269 — WELL LEAD ENDOTRACHEAL TUBE WITH EVACUATION LUMEN-ORAL
- K091516 — WELL LEAD SILICONE CATHETER WITH TEMPERATURE SENSOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.